Key result
Chemotherapy is linked to new-onset left ventricular diastolic dysfunction in ~10% of patients.
Why the study?
Cancer therapy-induced left ventricular diastolic dysfunction is an understudied potential early marker of cardiotoxicity in oncological settings.
Does cancer therapy induce early longitudinal changes in left ventricular diastolic function in patients without pre-existing cardiac disease?
Observational (n=60)
Does cancer therapy induce early longitudinal changes in left ventricular diastolic function in patients without pre-existing cardiac disease?
Cancer therapies can induce early left ventricular diastolic dysfunction that may present as either a transient or persistent condition, highlighting its potential role as an early marker of cardiotoxicity.
Answers are grounded in this paper and cite their sources.
May warrant diastolic monitoring during chemotherapy; leaves open whether this predicts HF or improves outcomes in larger trials.
Background Cancer therapy-induced left ventricular diastolic dysfunction (LVDD) is gaining research attention as a potential early marker of cardiotoxicity. Radiotherapy, chemotherapy, and targeted agents may cause cardiomyocyte energy depletion, cardiac fibrosis, and microvascular dysfunction—known mechanisms of diastolic dysfunction. Heart failure (HF) with preserved ejection fraction and LVDD remain understudied in oncological settings. Purpose We aimed to assess the changes in LV diastolic function caused by cancer treatment. Methods We prospectively enrolled 60 adults planned for chemotherapy (CT) for breast (n = 50) or gastrointestinal (n = 10) cancers. Exclusion criteria were fewer than 3 visits, a poor acoustic window, or pre-existing cardiac or chronic pulmonary disease. We performed 2D echocardiography at baseline and 1, 3, 6, 9, 12, and 18 months after CT initiation. Left ventricular ejection fraction (LVEF) was considered abnormal if it dropped by over 10% to below 50%. Longitudinal LV systolic dysfunction was defined as a decrease of over 15% to below 7 cm/s in systolic tissue S′ velocity, averaged from septal and lateral S′. We assessed LVDD using the 2025 American Society of Echocardiography algorithm and the parameters: indexed left atrial volume (LAVi); early (E) and late (A) mitral inflow velocities; E/A ratio; isovolumic relaxation time (IVRT); pulmonary artery systolic pressure (PASP); early diastolic tissue e′ velocity (average of septal and lateral e′) (LVe′); and E/e′ ratio. The temporal parameters' changes were estimated using generalised estimating equations (GEE) regression. Correlations were examined using the Spearman and chi-squared tests and Goodman-Kruskal's gamma (γ) statistic. Results The mean patient age was 53 years (SD 11.6), with 91.7% female. Half (n = 30) received anthracycline-based CT, either with or without trastuzumab; the remainder received non-anthracycline CT, with or without trastuzumab. The median CT duration was 98 days (IQR: 64, 112). Twenty-seven patients (45%) had radiotherapy. Over a median follow-up of 381 days (IQR: 187, 464), LVE/e' and LVe' declined significantly in the third month. Both parameters showed moderate correlation with LVS’ (Figure 1). Six patients had baseline LVDD; in one, it progressed from grade 1 to grade 2. New-onset LVDD occurred in 6 patients (10%), all grade 1 (Figure 2). Among them, two had transient LVDD; in two cases, LVDD advanced to grade 2, and one patient showed symptoms of HF (NYHA class II). There was a trend toward LVDD at the first and sixth months (Figure 2). No new-onset LVDD patient developed abnormal LVEF, although two had concurrent longitudinal systolic dysfunction. LVDD and longitudinal systolic dysfunction showed a positive association (ꭓ² = 5.2, p = 0.022; Kruskal’s γ = 0.64). Conclusions Cancer therapy-related LVDD may develop early and present as either a transient or persistent condition. Its clinical implications need further investigation.
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Slavcheva et al. (2026) conducted an observational in Breast or gastrointestinal cancer planned for chemotherapy (n=60). Chemotherapy vs. Baseline (pre-chemotherapy) was evaluated on New-onset left ventricular diastolic dysfunction (LVDD). Chemotherapy was associated with early decline in diastolic parameters and new-onset left ventricular diastolic dysfunction in 10% of patients, which correlated with systolic dysfunction (P=0.022).
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